RS1933891368 CLCN5

Health Risk Chr X:50086489
Upload your DNA to see your genotype for this variant.
Associated Conditions
Dent disease type 1
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
X-linked recessive nephrolithiasis with renal failure
Hypophosphatemic rickets
X-linked recessive
Dent disease type 1
Proteinuria
low molecular weight
with hypercalciuria and nephrocalcinosis
X-linked recessive nephrolithiasis with renal failure
Hypophosphatemic rickets
X-linked recessive
Other Variants in CLCN5
rs151340620 rs151340621 rs151340622 rs151340623 rs151340624 rs151340625 rs151340626 rs151340627 rs1569540520 rs151340628
Ask Dr. Hemsworth about this variant